Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45487359-45487515 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
chr21:45492507-45492564 | Rare:28; Clinvar (benign):2 | ||||
chr21:45562949-45563166 | Common:1; Rare:34 | ||||
chr21:46130038-46130182 | Common:2; Rare:62 | ||||
chr21:46243697-46243764 | Rare:24 | ||||
chr21:46374795-46375076 | Common:2; Rare:72 | ||||
chr21:46559568-46559623 | Rare:17 | ||||
chr22:17037144-17037297 | Common:2; Rare:31 | ||||
chr22:17968336-17968402 | Common:1; Rare:8 | ||||
chr22:18805454-18805672 | Rare:1 | ||||
chr22:19171606-19171729 | Rare:39 | ||||
chr22:19176448-19176586 | Rare:68; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:19361713-19362072 | Common:1; Rare:92 | ||||
chr22:19423129-19423354 | Rare:35 | ||||
chr22:19758620-19758791 | Rare:52 |